Cellular and Molecular Immunology · 2020 · 376 citations · 13 references
Life SciencesImmunologyInfectious DiseasesHost-pathogen InteractionsInnate ImmunityMolecular VirologyAntiviral ImmunityAntiviral TherapyInnate Immune ResponseInterferon ResponsesRig-i-like ReceptorsViral PathogenesisAntiviral Interferon ResponsesHost Antiviral ResponseInhibition Of Interferon ResponsesInterferon Response To Viral InfectionMitochondrial Antiviral SignalingRig-i SignalingType I Interferon InductionType I Interferon Responses
COVID-19 is caused by SARS-CoV-2. 1 As of July 16th, 2020, there were 13,579,581 diagnosed cases and 584,782 deaths attributed to COVID-19 reported globally ( https://coronavirus.jhu.edu/map.html ). 2 Unfortunately, there is still no effective drug or vaccine for treating this disease. To accelerate drug development, there is an urgent need to identify critical molecular targets and the role they play in infection. Herein, we reported that Orf9b localizes on the membrane of mitochondria and suppresses type I interferon (IFN-I) responses through association with TOM70, and TOM70 overexpression could largely rescue this inhibition. Our results suggest the potential of targeting Orf9b-TOM70 interaction as a novel therapeutic strategy of COVID-19.
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A SARS-CoV-2 protein interaction map reveals targets for drug repurposing
David E. Gordon, Gwendolyn Μ. Jang, Mehdi Bouhaddou et al. · Nature · 2020 · 4.9K citations · Full text
Imbalanced Host Response to SARS-CoV-2 Drives Development of COVID-19
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SARS-CoV-2 productively infects human gut enterocytes
Mart M. Lamers, Joep Beumer, Jelte van der Vaart et al. · Science · 2020 · 1.7K citations · Full text
Lactate Is a Natural Suppressor of RLR Signaling by Targeting MAVS
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